Simon C Langton Hewer
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View article: Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis
Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis Open
We found that nebulised antibiotics, alone or with oral antibiotics, were better than no treatment for early infection with P aeruginosa. Eradication may be sustained in the short term. There is insufficient evidence to determine whether t…
View article: Dietary interventions for managing glucose abnormalities in people with cystic fibrosis
Dietary interventions for managing glucose abnormalities in people with cystic fibrosis Open
This is a protocol for a Cochrane Review (intervention). The objectives are as follows: To assess the effects of dietary interventions on glycaemic control and clinical status in people with cystic fibrosis who have dysglycaemia.
View article: Intravenous or oral antibiotic treatment in adults and children with cystic fibrosis and Pseudomonas aeruginosa infection: the TORPEDO-CF RCT
Intravenous or oral antibiotic treatment in adults and children with cystic fibrosis and Pseudomonas aeruginosa infection: the TORPEDO-CF RCT Open
Background People with cystic fibrosis are susceptible to pulmonary infection with Pseudomonas aeruginosa . This may become chronic and lead to increased mortality and morbidity. If treatment is commenced promptly, infection may be eradica…
View article: Children’s charter for lung health
Children’s charter for lung health Open
Every child and young person has the right to breathe clean air, with healthy lungs. Pre-conception, in utero and early life conditions affect children’s lungs, their lung growth and their long-term health. Government, societal and individ…
View article: A breathless teenager
A breathless teenager Open
In children with persistent chylothoraces of unknown origin, intranodal lymphangiography can be used to help identify the source of a leak. This may enable embolisation with glue and coils to enable resolution of the chylothoraces. …
View article: Intravenous versus oral antibiotics for eradication of Pseudomonas aeruginosa in cystic fibrosis (TORPEDO-CF): a randomised controlled trial
Intravenous versus oral antibiotics for eradication of Pseudomonas aeruginosa in cystic fibrosis (TORPEDO-CF): a randomised controlled trial Open
National Institute for Health Research Health Technology Assessment Programme.
View article: The ERS approach to e-cigarettes is entirely rational
The ERS approach to e-cigarettes is entirely rational Open
“This is an author-submitted, peer-reviewed version of a manuscript that has been accepted for publication in the European Respiratory Journal, prior to copy-editing, formatting and typesetting. This version of the manuscript may not be du…
View article: Technique, pitfalls, quality, radiation dose and findings of dynamic 4-dimensional computed tomography for airway imaging in infants and children
Technique, pitfalls, quality, radiation dose and findings of dynamic 4-dimensional computed tomography for airway imaging in infants and children Open
View article: Referee report. For: Case Report: First report of Elizabethkingia miricola infection in a patient with cystic fibrosis [version 1; referees: 1 approved with reservations]
Referee report. For: Case Report: First report of Elizabethkingia miricola infection in a patient with cystic fibrosis [version 1; referees: 1 approved with reservations] Open
View article: Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis
Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis Open
Respiratory tract infection with Pseudomonas aeruginosa occurs in most people with cystic fibrosis. Once chronic infection is established, Pseudomonas aeruginosa is virtually impossible to eradicate and is associated with increased mortali…
View article: Pancreatic cystosis in cystic fibrosis
Pancreatic cystosis in cystic fibrosis Open
A 17-year-old boy was diagnosed with cystic fibrosis at age 6 years.Genetic analysis revealed homozygous ΔF508 mutations.His first abdominal ultrasound was performed in March 2012 as part of the annual cystic fibrosis review.This demonstra…